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3-Chloro-4-Fluorobenzylamine

    • Product Name 3-Chloro-4-Fluorobenzylamine
    • Alias 3-chloro-4-fluorobenzenemethanamine
    • Einecs 643-824-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    805424

    Product Name 3-Chloro-4-Fluorobenzylamine
    Cas Number 861166-51-6
    Molecular Formula C7H7ClFN
    Molecular Weight 159.59
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥98%
    Boiling Point 235-237°C
    Density 1.26 g/cm³ (approximate)
    Solubility Soluble in organic solvents like DMSO and methanol
    Refractive Index 1.572 (approximate)
    Storage Conditions Store at 2-8°C, tightly sealed
    Smiles NCc1ccc(Cl)c(F)c1
    Inchi InChI=1S/C7H7ClFN/c8-6-3-1-2-5(4-10)7(6)9
    Synonyms 1-(3-Chloro-4-fluorophenyl)methanamine

    As an accredited 3-Chloro-4-Fluorobenzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3-Chloro-4-Fluorobenzylamine, sealed with a screw cap and labeled with hazard warnings.
    Shipping 3-Chloro-4-Fluorobenzylamine is shipped in tightly sealed containers under inert atmosphere to prevent contamination and degradation. The packaging complies with international regulations for hazardous chemicals. During transit, it is protected from extreme temperatures, light, and moisture. Proper labeling and documentation ensure safe and regulated handling throughout shipping.
    Storage Store 3-Chloro-4-Fluorobenzylamine in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as oxidizing agents and strong acids. Protect from light and moisture. Keep the storage area clearly labeled and secured, and ensure it is accessible only to trained personnel. Follow all local regulations and recommended safety practices for storage of hazardous chemicals.
    Application of 3-Chloro-4-Fluorobenzylamine

    Applications of 3-Chloro-4-Fluorobenzylamine in Industrial Manufacturing

    3-Chloro-4-Fluorobenzylamine serves as a crucial intermediate in several sectors where selective benzylic amines with halogen substitutions are necessary. As the direct manufacturer, we support integrated custom syntheses for major pharmaceutical, agrochemical, pigment, and specialty chemical producers worldwide. Below, we present key industrial application scenarios grounded in real downstream markets.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    In regulated pharmaceutical manufacturing, 3-Chloro-4-Fluorobenzylamine acts as a benzylamine source for amide and urea scaffold formation in small molecule drug APIs. Major multinational pharma companies deploy this raw material in staged processes for CNS, anti-infective, and oncology drug fabrication. Controlled batch and continuous flow integrations depend on high-purity supply to align with ICH Q7 and regional GMP protocols, supporting the integrity of finished actives.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA)
    • EU Guidelines for Good Manufacturing Practice for Medicinal Products
    • Chinese Pharmacopoeia guidance for chemical API intermediates

    Typical usage ratio

    • 0.6–1.5 molar equivalents per target API precursor, calibrated by process chemists based on desired conversion and impurity profile

    Downstream process integration

    • Introduced in amidation, reductive amination, or nucleophilic substitution steps to construct final heterocyclic or aromatic API scaffolds

    Final product types

    • Small molecule APIs for CNS disorders
    • Targeted oncology drugs
    • Oral solid dose antibiotics
    • Bulk pharmaceutical intermediates for contract manufacturing organizations (CMOs)

    2. Agrochemical Herbicide and Fungicide Intermediate

    Our downstream partners in crop production harness this material for custom syntheses of substituted benzylamide motifs in new generation herbicide and fungicide actives. Process managers adjust charge ratios in closed, solvent-optimized reactors, following chemical registration requirements under global agrochemical control regimes. Consistent halogenation on the aromatic ring supports active ingredient selectivity in post-emergent and seed treatment products.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • REACH Regulation (EC) No. 1907/2006
    • EPA FIFRA (US) Pesticide Registration Guidelines
    • Chinese National Standards for Pesticide Raw Materials (GB 4839-2008)

    Typical usage ratio

    • 0.8–1.2 equivalents relative to chlorinated acyl precursors; optimization based on active ingredient yield goals and waste stream minimization

    Downstream process integration

    • Participates in condensation and acylation reactions during the formation of final biologically active pyridine, triazole, or benzamide structures

    Final product types

    • Herbicide actives for cereals and oilseed crops
    • Systemic fungicides for high-value fruits and vegetables
    • Intermediate stage technical concentrates
    • Custom-formulated pesticide premixes

    3. Dye and Pigment Intermediate Manufacturing

    Leading pigment houses utilize this amine as a coupling or nucleophile unit in the synthesis of fluorinated azo and benzyl-pyridine dyes. Controlled addition ensures precise color hue development and improved fade resistance for high-grade industrial coatings and polymer colorants. Raw material verification is essential to ensure conformance to EN ISO pigment manufacturing protocols and environmental safety schemes for downstream application in plastics and inks.

    Industry compliance standards

    • EN ISO 1248:2020 Pigments & Extenders—General Methods of Testing
    • OEKO-TEX Eco Passport for textile chemical compliance
    • REACH Annex XVII restrictions (EU)
    • Directive 2008/105/EC on Environmental Quality Standards

    Typical usage ratio

    • 2–10% by mass as coupling component in total dye or pigment batch formulation; adjusted for depth and purity of target shades

    Downstream process integration

    • Charged during pigment synthesis after diazotization or as nucleophile in aromatic substitution for colorfast dye development

    Final product types

    • Industrial pigment dispersions
    • Plastic and polymer masterbatches
    • High-performance printing inks
    • Textile dye colorants for technical fabrics

    4. Custom Fine Chemical Synthesis for Specialty Additives

    Specialty chemical companies select this raw material for pathway-specific syntheses, including UV absorber precursors, halogenated stabilizers, and performance additives used in lubricants and engineered coatings. Production lines apply tightly controlled stoichiometry using in-line analytical monitoring, reflecting advanced QA requirements under ISO 9001 and downstream sector standards. Integration efficiency ensures final product compliance with customer technical dossiers and regulatory approvals.

    Industry compliance standards

    • ISO 9001 Certified Quality Management
    • ASTM D6046 Standard for UV Stabilizers and Additives
    • RoHS Compliance (EU Directive 2011/65/EU) for electronics applications
    • TSCA Inventory Status (US EPA)

    Typical usage ratio

    • 5–25% relative to other intermediate building blocks; final charge determined by functional group density and required additive performance

    Downstream process integration

    • Feedstock for closed-reactor synthesis of UV absorbers or stabilizing agents, introduced post-initial aryl activation step

    Final product types

    • UV stabilizers for plastics and paints
    • Electronic coating intermediates
    • Lubricant formulation additives
    • Specialty polymer modifiers
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    Certification & Compliance
    More Introduction

    3-Chloro-4-Fluorobenzylamine: A Chemical Manufacturer’s Perspective

    Understanding the Chemistry Behind 3-Chloro-4-Fluorobenzylamine

    From the production floor, 3-Chloro-4-Fluorobenzylamine stands out for its unique molecular structure and its practical attributes in advanced synthetic applications. We synthesize it using precision methodologies rooted in decades of fine chemical manufacturing. Its formula, C7H7ClFN, reflects two distinct halogen substitutions on the benzene ring, giving it reliable reactivity and selectivity compared to less substituted benzylamine analogs.

    In our plant, maintaining consistent product quality starts with the careful selection of raw fluorobenzene and chlorinated reagents that meet stringent purity checks. Through controlled amination and halogenation steps, any batch inconsistencies become immediately obvious, so our approach always emphasizes real-time monitoring and post-synthesis analysis by NMR, HPLC, and GC techniques. Chlorine at the third ring position and fluorine at the fourth change both the chemical’s electronic properties and the kinds of downstream molecules it helps build.

    Compared to unsubstituted benzylamines, this compound brings distinct advantages for synthetic organic chemists. The electron-withdrawing nature of chlorines and fluorines prevents side reactions during alkylation or acylation, which makes the process more predictable on a bigger scale. Our customers in pharmaceutical R&D projects tell us this enables them to target niche molecules that would remain out of reach using traditional benzylamine derivatives.

    Specifications and Purity at Industrial Scale

    Quality assurance begins long before the product leaves the reactor. We work with analytical teams who focus on purity levels above 99% for each shipment of 3-Chloro-4-Fluorobenzylamine. Moisture, trace solvent, and heavy metal content are all measured with validated analytical methods. Each kilo passes a thick stack of documentation—material origin, reaction logs, chromatograms, and test certificates. Anything less would undermine confidence from partners who base multi-step routes on our chemical input.

    Over the years, experience has taught that certain specification details matter much more than flashy technical terms. Color, odor, and solution stability can flag production issues even before analytical reports arrive. In the warehouse, finished batches cool under nitrogen to prevent oxidation. We use amber glass or PTFE-lined drums for all shipments, because we’ve noticed that ordinary HDPE does not prevent gradual contamination or slow discoloration. We transport with temperature monitoring, since modest heat spikes sometimes shorten the shelf life and change reactivity for critical uses.

    A hydrophilic amine group offers certain solubility features in polar solvents. The precise 3-chloro and 4-fluoro substitutions influence melting and boiling points enough that our clients find this version handier in multi-solvent protocols than single-halogenated benzylamines. Direct feedback comes in through pilot projects, where a slight structural tweak can save weeks in downstream separations or purification. We actively encourage partner labs to share back their process quirks, and our own improvements to particle size control and liquid purity keep pace with their demands.

    Production Know-how and Scale-up Considerations

    Our production of 3-Chloro-4-Fluorobenzylamine is not simply a recipe, but a reflection of practical problem-solving. On a pilot line, subtle process shifts—like agitation speed and order of addition—change yields and impurity profiles. The biggest learning moments come from scaling-up. At lab scale, a crystal-clear product is easy; reaching hundreds of kilos means controlling for exothermicity during amination, precise reagent dosing, and rigorous drying of intermediates. Many technical details, like nitrogen purging during chlorination or selecting catalysts that avoid heavy-metal contamination, come from direct on-site experience.

    Our investment in glass-lined vessels prevents corrosion from aggressive starting materials, and the entire process uses closed systems for both safety and product stability. Product loss control means more than just efficiency. The alternative—a yield drop or off-spec batch—delays everything downstream, costing time and trust. With 3-Chloro-4-Fluorobenzylamine, a subpar batch could spoil sensitive syntheses in API or agrochemical intermediate manufacturing, so routine in-process monitoring is a core factory discipline.

    Over years of repeated synthesis, we refined purification. At first, we struggled with trace residues from starting materials, but process tweaks with mixed-solvent recrystallization and multi-stage filtration reduced side-product buildup. After shifting from older distillation setups to wiped-film evaporation, we could recover product with minimal decomposition. These lessons came only with repeated hands-on trials, not just from literature.

    Use Cases in Research and Industrial Pipelines

    Research teams approach us mainly for the reliability of our 3-Chloro-4-Fluorobenzylamine in producing functionalized intermediates for drug candidates. One example comes from a long-term pharmaceutical partner developing kinase inhibitors. Early efforts with monochloro- or monofluoro-substituted benzylamines often delivered poor yields due to unwanted side-chain reactions, but our dual-halogenated product gave them sharper selectivity during coupling to carbo- or heterocyclic scaffolds. Real data from their syntheses showed measurable improvements in purity and batch-to-batch reproducibility, speeding up candidate progression.

    Agrochemical producers cite different priorities. For them, shelf stability under variable warehouse conditions—humid days, sporadic high temperatures—takes center stage. Here, our tightly sealed packaging and batch-specific COAs give them confidence that each drum arrives within tight impurity levels, ready for formulation or direct downstream reactions. Some collaborators report using 3-Chloro-4-Fluorobenzylamine as a precursor to advanced pyridine derivatives, which are useful for crop protection chemicals that require tight impurity controls because regulatory approvals rest on those trace-level details.

    In material science applications, our compound sometimes acts as a surface-modifying agent for specialty polymers or as a niche additive in electronic materials, where halogen content influences final conductivity or chemical resistance. For these clients, we provide a different service—matching residual salt profiles to their impedance standards. Our technical team communicates with their process chemists to nail down these little details.

    Differences from Other Benzylamines

    Not all benzylamines behave the same in complex synthesis. Chemists who rely on off-the-shelf benzylamine or mono-halogenated versions often see reaction bottlenecks in key steps—especially where undesired side products dominate. Our hands-on history with 3-Chloro-4-Fluorobenzylamine highlights how subtle substitution changes translate to tangible process benefits.

    Electron-withdrawing halogens at both the third and fourth positions alter not just reactivity, but also the compound’s safety profile and environmental behavior. This twin substitution slows certain oxidative degradation pathways, giving longer shelf life in ambient storage. It also means better resistance to ambient light or trace metal contamination, critical for high-value applications. Our internal testing—regular sunlight exposure and accelerated aging—tracks color and odor changes over time, showing clear differences against less-substituted alternatives.

    Selecting between various benzylamine analogs demands an understanding of target product needs. Where chemoselectivity matters, the 3-chloro-4-fluoro combination unlocks challenging transformations. Chemists use this product to introduce functional groups in precise positions on complex aromatic systems, sidestepping many purification problems that would plague unsubstituted or singly halogenated precursors. We share these hands-on stories not as abstract use cases, but as accumulated experience from years of troubleshooting.

    Process safety also gets attention. Our dual-substituted product brings a higher threshold for certain exothermic decomposition reactions during heated transformations—a feature less pronounced in mono-halogenated compounds. Feedback from partner labs resonates with our own findings: cleaner reactions, less waste, and smoother scale-up, especially in hydrogenation or reductive amination steps.

    Challenges in Production and Distribution

    Making 3-Chloro-4-Fluorobenzylamine at scale demands more than following a published protocol. Some hurdles come from raw material variability—outsourced fluorobenzenes can fluctuate in trace impurity levels. Over the years, shifting to direct supplier relationships and in-house purification kept our input streams consistent. Even then, small shifts in solvent quality led to unwanted byproducts, prompting new quality audits.

    Transportation stands as another challenge. Benzylamines in general show sensitivity to air and light, especially in bulk. Early on, shipments with slight exposure suffered from increased color, higher amine degradation, and, in rare cases, pressure build-up. We brought packaging in-house and adopted multilayered, lightblock solutions. Customers trading on the old open-drum standard quickly saw the difference.

    Regulatory environments evolve annually. For every new regulatory requirement, we upgrade our documentation pipeline. Analytical proofs, stability studies, and impurity dossiers keep our product ready for scrutiny from our chemical and pharmaceutical partners. We weave these updates into daily operations, and strengthen them with on-site QA training to embed compliance into every batch, not just on paper.

    Even after years of refining the production process, unexpected equipment maintenance or regional power outages can halt things mid-stream. Redundant line capacity and cross-training among operators ensure that schedules stay predictable. Our site technicians constantly review energy loads and backup generator uptime, lessons learned from living through several infrastructure failures.

    Environmental and Safety Considerations

    As a chemical manufacturer, we never overlook the environmental impact. Halogenated amines, in the wrong hands, can be persistent in the environment or cause disposal problems. Our plant features closed-loop waste capture and on-site neutralization, so nothing leaves the facility untreated. Scrubbing systems and regular waste audits give us a real sense of the downstream burden, not just for public reporting, but to preserve long-term operational licenses and the trust of our local community.

    Each operator on the line undergoes solvent handling, spill response, and personal exposure training. We learned long ago that strong smells or minor skin irritation from amine vapors signal deeper issues in process sealing or ventilation. Air monitoring and personal protective equipment cut incident risk, but real safety culture comes from active reporting of any oddity, no matter how small.

    Warehouse teams document every storage move. Early on, the industry learned too many lessons from overlooked leaks or improper stacking of drums. Now, our inventory tracking and environmental monitoring let us pinpoint the source of any issue, whether it’s a temperature excursion or trace vapor detection in secondary containment. This attention to detail allows us to keep both product quality and worker safety high.

    Solutions for Industry Users

    For process chemists and production managers, the biggest headaches come from batch variability, inconsistent supply, and unclear impurity profiles. Over hundreds of shipments, our reliability springs not from luck, but from routine double-checks and willingness to pause for investigation. If a batch trends toward an unexpected impurity, we rerun analytics before shipping. Many customers appreciate frank conversations and transparent supply chain updates, instead of silence and stockouts.

    Some biotech and specialty chemical labs push our product to the edge—demanding non-standard solvent blends or higher crystallinity for unusual reactor setups. We respond with real-time technical support, offering sample granulations or custom filtering, when possible, to meet those niche preferences. Instead of rigid one-size-fits-all processes, we treat every technical challenge as an invitation to learn.

    Shipping smaller, pre-tested lots to new clients gives them direct data while de-risking their own development pipelines. Some of our best collaborators started with a single kilogram, only to return with multi-ton requests once they validated the compound in real-world syntheses. These relationships grow not from formal contracts, but from meeting genuine process demands and troubleshooting alongside customer chemists.

    The Path Forward: Listening, Learning, and Adapting

    Manufacturing 3-Chloro-4-Fluorobenzylamine at scale highlights the value of lived experience in bulk chemical supply. Years on the floor taught us how to minimize loss, head off process upsets, and uncover tiny sources of impurity that stunt complex syntheses. For those on the receiving end, assurance comes from transparency, regular performance validation, and open dialogue about shifting needs.

    Feedback cycles with end users drive continuous process improvements. Some customers find novel uses for this molecule in completely unexpected branches of synthesis—antiviral research, dye manufacture, or polymer surface treatment. Each conversation opens new ways to adjust our batch protocols, initiate pilot runs, or test new packaging methods for unique supply chains.

    We encourage researchers and industrial chemists to treat us not just as a supplier, but as an active partner. In every kilo of 3-Chloro-4-Fluorobenzylamine shipped, a legacy of hands-on effort, method refinement, and deep commitment to quality comes standard. Meeting tough industry problems head-on keeps us sharp and our product at the leading edge, ready for the next generation of chemical breakthroughs.